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rs180177131

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 7 Fanconi anemia, complementation group N
(-;C) 3 increased risk of breast cancer
(C;C) 0 common in clinvar
ReferenceGRCh38 38.1/141
Chromosome16
Position23621449
GenePALB2
is asnp
is mentioned by
dbSNPrs180177131
ebirs180177131
HLIrs180177131
Exacrs180177131
Varsomers180177131
Maprs180177131
PheGenIrs180177131
hapmaprs180177131
1000 genomesrs180177131
hgdprs180177131
ensemblrs180177131
gopubmedrs180177131
geneviewrs180177131
scholarrs180177131
googlers180177131
pharmgkbrs180177131
gwascentralrs180177131
openSNPrs180177131
23andMers180177131
23andMe allrs180177131
SNP Nexus

SNPshotrs180177131
SNPdbers180177131
MSV3drs180177131
GWAS Ctlgrs180177131
Max Magnitude7
ClinVar
Risk rs180177131(;)
Alt rs180177131(;)
Reference rs180177131(C;C)
Significance Pathogenic
Disease Familial cancer of breast not provided Hereditary cancer-predisposing syndrome
Variation info
Gene PALB2
CLNDBN Familial cancer of breast not provided Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000016.9:g.23632770delG
CLNSRC PALB2 database
CLNACC RCV000114586.2, RCV000133484.1, RCV000160811.1,


[PMID 21285249OA-icon.png] Contribution of inherited mutations in the BRCA2-interacting protein PALB2 to familial breast cancer.